PARD3B-SLC40A1 Fusion FISH Probe
The PARD3B-SLC40A1 Fusion FISH Probe is used to confirm a fusion of the PARD3B and SLC40A1 genes. The fusion of the PARD3B and SLC40A1 genes has been associated with Uveal Melanoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| PARD3B-SLC40A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-RERE | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-REOR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-REGO | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-REGR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-REAQ | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-ORRE | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-OROR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-ORGO | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GORE | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GOOR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GOGO | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GOGR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GRRE | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GROR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GRGO | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GRGR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-AQRE | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-AQOR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-AQGO | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-AQGR | 20 (40 μL) | 200 μL |
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| PARD3B-SLC40A1-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC40A1 Gene Summary
The protein encoded by this gene is a cell membrane protein that may be involved in iron export from duodenal epithelial cells. Defects in this gene are a cause of hemochromatosis type 4 (HFE4). [provided by RefSeq, Jul 2008]
Gene Name: Solute Carrier Family 40 Member 1
Chromosome: CHR2: 190425315 -190445537
Locus: 2q32.2
PARD3B Gene Summary
The Par-3 Family Cell Polarity Regulator Beta (PARD3B) gene is located on chr2 :205410515-206484886 at 2q33.3.
Gene Name: Par-3 Family Cell Polarity Regulator Beta
Chromosome: CHR2: 205410515 -206484886
Locus: 2q33.3
Gene Diseases
The PARD3B SLC40A1 Fusion has been associated with the following diseases:
| Disease Name |
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| Uveal Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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